OR2L13
gene geneOn this page
Summary
OR2L13 (olfactory receptor family 2 subfamily L member 13, HGNC:19578) is a protein-coding gene on chromosome 1q44, encoding Olfactory receptor 2L13 (Q8N349). Odorant receptor.
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome.
Source: NCBI Gene 284521 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 209 total
- MANE Select transcript:
NM_001395936
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:19578 |
| Approved symbol | OR2L13 |
| Name | olfactory receptor family 2 subfamily L member 13 |
| Location | 1q44 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000196071 |
| Ensembl biotype | protein_coding |
| Entrez | 284521 |
Gene structure
Transcript identifiers
Ensembl transcripts: 3 — 3 protein_coding
ENST00000358120, ENST00000641714, ENST00000641893
RefSeq mRNA: 3 — MANE Select: NM_001395936
NM_001304535, NM_001395936, NM_175911
CCDS: CCDS1637
Canonical transcript exons
ENST00000358120 — 3 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001441816 | 248098651 | 248098775 |
| ENSE00003812202 | 248095184 | 248095254 |
| ENSE00003978245 | 248099358 | 248101163 |
Expression profiles
Bgee: expression breadth broad, 70 present calls, max score 76.66.
FANTOM5 (CAGE): breadth broad, TPM avg 1.0371 / max 82.5033, expressed in 271 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 9651 | 1.0371 | 271 |
Top tissues by expression
211 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| prefrontal cortex | UBERON:0000451 | 76.66 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 75.54 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 72.62 | gold quality |
| spinal cord | UBERON:0002240 | 72.50 | gold quality |
| frontal cortex | UBERON:0001870 | 68.46 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 67.85 | gold quality |
| hypothalamus | UBERON:0001898 | 67.69 | gold quality |
| endothelial cell | CL:0000115 | 67.63 | silver quality |
| neocortex | UBERON:0001950 | 67.49 | gold quality |
| right frontal lobe | UBERON:0002810 | 66.06 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 65.80 | gold quality |
| cortical plate | UBERON:0005343 | 65.74 | gold quality |
| cerebral cortex | UBERON:0000956 | 64.49 | gold quality |
| substantia nigra | UBERON:0002038 | 63.97 | gold quality |
| primary visual cortex | UBERON:0002436 | 63.90 | gold quality |
| putamen | UBERON:0001874 | 63.11 | gold quality |
| caudate nucleus | UBERON:0001873 | 62.22 | gold quality |
| nucleus accumbens | UBERON:0001882 | 62.13 | gold quality |
| forebrain | UBERON:0001890 | 61.59 | gold quality |
| amygdala | UBERON:0001876 | 61.46 | gold quality |
| midbrain | UBERON:0001891 | 61.21 | gold quality |
| ventricular zone | UBERON:0003053 | 61.10 | gold quality |
| brain | UBERON:0000955 | 60.29 | gold quality |
| Ammon’s horn | UBERON:0001954 | 59.85 | gold quality |
| occipital lobe | UBERON:0002021 | 59.36 | gold quality |
| lower lobe of lung | UBERON:0008949 | 58.11 | silver quality |
| superior frontal gyrus | UBERON:0002661 | 55.58 | gold quality |
| Brodmann (1909) area 46 | UBERON:0006483 | 55.45 | silver quality |
| temporal lobe | UBERON:0001871 | 54.84 | gold quality |
| cerebellar cortex | UBERON:0002129 | 54.33 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.62 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
46 targeting OR2L13, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-656-3P | 100.00 | 72.15 | 2788 |
| HSA-MIR-5692B | 100.00 | 71.32 | 2622 |
| HSA-MIR-5692C | 100.00 | 71.32 | 2622 |
| HSA-MIR-1277-5P | 100.00 | 73.95 | 5056 |
| HSA-MIR-4482-3P | 99.98 | 72.50 | 3147 |
| HSA-MIR-548AN | 99.97 | 70.91 | 2817 |
| HSA-MIR-495-3P | 99.96 | 72.81 | 4197 |
| HSA-MIR-5688 | 99.96 | 73.23 | 4504 |
| HSA-MIR-590-3P | 99.96 | 74.34 | 6478 |
| HSA-LET-7C-3P | 99.95 | 73.42 | 2862 |
| HSA-MIR-381-3P | 99.93 | 71.87 | 2854 |
| HSA-MIR-3143 | 99.93 | 71.96 | 3104 |
| HSA-MIR-300 | 99.92 | 71.76 | 2856 |
| HSA-MIR-7-1-3P | 99.91 | 71.53 | 4384 |
| HSA-MIR-7-2-3P | 99.91 | 71.40 | 4394 |
| HSA-MIR-380-3P | 99.89 | 70.18 | 1978 |
| HSA-MIR-30A-3P | 99.87 | 69.74 | 2928 |
| HSA-MIR-30D-3P | 99.87 | 69.92 | 2917 |
| HSA-MIR-30E-3P | 99.87 | 69.68 | 2942 |
| HSA-MIR-2052 | 99.79 | 69.37 | 2031 |
| HSA-MIR-448 | 99.79 | 72.37 | 2103 |
| HSA-MIR-12129 | 99.72 | 67.45 | 1311 |
| HSA-MIR-2053 | 99.57 | 69.15 | 1635 |
| HSA-MIR-7159-3P | 99.51 | 70.17 | 1920 |
| HSA-MIR-4643 | 99.49 | 67.63 | 1791 |
| HSA-MIR-203A-3P | 99.49 | 70.56 | 2806 |
| HSA-MIR-183-3P | 99.41 | 69.41 | 1598 |
| HSA-MIR-889-3P | 99.40 | 69.76 | 2103 |
| HSA-MIR-4797-5P | 99.39 | 68.01 | 1354 |
| HSA-MIR-16-2-3P | 99.29 | 70.60 | 1954 |
Literature-anchored findings (GeneRIF, showing 2)
- RNA-Seq evidence of testis-specific monoallelic expression of OR2L13, located 419 kb downstream of the GCSAML somatic (secondary), imprinted differentially methylated region (iDMR). OR2L13 has a predicted CGI-bearing allelically methylated region overlapping the promoter region in blood, spleen, lung, liver, esophagus, and brain, but hypomethylated in gamete, blastocyst, placenta, thymus, and spinal cord methylomes. (PMID:29545821)
- Platelet olfactory receptor activation limits platelet reactivity and growth of aortic aneurysms. (PMID:35324479)
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Or2l13 | ENSMUSG00000056822 |
| mus_musculus | Or2l13b | ENSMUSG00000061361 |
| rattus_norvegicus | Or2l13c | ENSRNOG00000074249 |
| rattus_norvegicus | Or2l13 | ENSRNOG00000074329 |
Paralogs (92): OR2B6 (ENSG00000124657), OR13C9 (ENSG00000136839), OR13C4 (ENSG00000148136), OR2M5 (ENSG00000162727), OR10A5 (ENSG00000166363), OR2D2 (ENSG00000166368), OR2B2 (ENSG00000168131), OR2C1 (ENSG00000168158), OR13J1 (ENSG00000168828), OR10G3 (ENSG00000169208), OR10A3 (ENSG00000170683), OR10A4 (ENSG00000170782), OR10A2 (ENSG00000170790), OR13H1 (ENSG00000171054), OR2K2 (ENSG00000171133), OR2M4 (ENSG00000171180), OR10H2 (ENSG00000171942), OR10H5 (ENSG00000172519), OR10AD1 (ENSG00000172640), OR2Y1 (ENSG00000174339), OR10AG1 (ENSG00000174970), OR2T1 (ENSG00000175143), OR10P1 (ENSG00000175398), OR2T35 (ENSG00000177151), OR2M7 (ENSG00000177186), OR2T12 (ENSG00000177201), OR2T33 (ENSG00000177212), OR2AJ1 (ENSG00000177275), OR2T8 (ENSG00000177462), OR2G3 (ENSG00000177476), OR2G2 (ENSG00000177489), OR2B11 (ENSG00000177535), OR2D3 (ENSG00000178358), OR13D1 (ENSG00000179055), OR10A7 (ENSG00000179919), OR2Z1 (ENSG00000181733), OR2V2 (ENSG00000182613), OR10G7 (ENSG00000182634), OR2T29 (ENSG00000182783), OR2T34 (ENSG00000183310)
Protein
Protein identifiers
Olfactory receptor 2L13 — Q8N349 (reviewed: Q8N349)
Alternative names: Olfactory receptor 2L14
All UniProt accessions (2): A0A126GW96, Q8N349
UniProt curated annotations — full annotation on UniProt →
Function. Odorant receptor.
Subcellular location. Cell membrane.
Similarity. Belongs to the G-protein coupled receptor 1 family.
RefSeq proteins (3): NP_001291464, NP_001382865, NP_787107 (=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000276 | GPCR_Rhodpsn | Family |
| IPR000725 | Olfact_rcpt | Family |
| IPR017452 | GPCR_Rhodpsn_7TM | Domain |
Pfam: PF13853
UniProt features (21 total): topological domain 8, transmembrane region 7, glycosylation site 2, sequence variant 2, chain 1, disulfide bond 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q8N349-F1 | 89.83 | 0.72 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Disulfide bonds (1): 96–188
Glycosylation sites (2): 5, 20
Function
Pathways and Gene Ontology
Reactome pathways
2 pathways
| ID | Pathway |
|---|---|
| R-HSA-381753 | Olfactory Signaling Pathway |
| R-HSA-9752946 | Expression and translocation of olfactory receptors |
MSigDB gene sets: 58 (showing top):
GSE45365_CTRL_VS_MCMV_INFECTION_NK_CELL_DN, RNGTGGGC_UNKNOWN, GCANCTGNY_MYOD_Q6, GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, AAAYRNCTG_UNKNOWN, CAGCTG_AP4_Q5, PAX2_01, KEGG_OLFACTORY_TRANSDUCTION, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, RFX1_02, chr1q44, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, PITX2_Q2, GOMF_OLFACTORY_RECEPTOR_ACTIVITY
GO Biological Process (4): detection of chemical stimulus involved in sensory perception of smell (GO:0050911), signal transduction (GO:0007165), G protein-coupled receptor signaling pathway (GO:0007186), sensory perception of smell (GO:0007608)
GO Molecular Function (3): G protein-coupled receptor activity (GO:0004930), olfactory receptor activity (GO:0004984), protein binding (GO:0005515)
GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)
Reactome top-level categories
Rollup of top-2 pathways:
| Category | Pathways |
|---|---|
| Sensory Perception | 1 |
| Olfactory Signaling Pathway | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| transmembrane signaling receptor activity | 2 |
| sensory perception of smell | 1 |
| detection of chemical stimulus involved in sensory perception | 1 |
| cell communication | 1 |
| cellular process | 1 |
| signaling | 1 |
| regulation of cellular process | 1 |
| cellular response to stimulus | 1 |
| G protein-coupled receptor activity | 1 |
| signal transduction | 1 |
| sensory perception of chemical stimulus | 1 |
| G protein-coupled receptor signaling pathway | 1 |
| detection of chemical stimulus involved in sensory perception of smell | 1 |
| binding | 1 |
| membrane | 1 |
| cell periphery | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
602 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| OR2L13 | C11orf21 | Q9P2W6 | 583 |
| OR2L13 | TAS2R50 | P59544 | 573 |
| OR2L13 | TAS2R13 | Q9NYV9 | 541 |
| OR2L13 | C14orf119 | Q9NWQ9 | 507 |
| OR2L13 | TAS2R5 | Q9NYW4 | 506 |
| OR2L13 | B3KSW5 | B3KSW5 | 476 |
| OR2L13 | RNF167 | Q9H6Y7 | 475 |
| OR2L13 | PRKG1 | P14619 | 449 |
| OR2L13 | FAM181A | Q8N9Y4 | 433 |
| OR2L13 | TAS2R10 | Q9NYW0 | 432 |
| OR2L13 | PYROXD1 | Q8WU10 | 420 |
| OR2L13 | CACNA2D3 | Q8IZS8 | 415 |
| OR2L13 | OR2C1 | O95371 | 412 |
| OR2L13 | OR1J2 | Q8NGS2 | 407 |
| OR2L13 | TSPAN32 | Q96QS1 | 402 |
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| OR2L13 | SERPINA1 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (6): SERPINA1 (Affinity Capture-MS), ALB (Affinity Capture-MS), CDSN (Affinity Capture-MS), IGHG3 (Affinity Capture-MS), GPX7 (Affinity Capture-MS), OR2L13 (Two-hybrid)
ESM2 similar proteins: A3KFT3, P0C628, P34982, P34985, P37068, P37071, Q15612, Q60879, Q8N146, Q8N162, Q8N349, Q8NG80, Q8NG81, Q8NG83, Q8NG85, Q8NG92, Q8NG95, Q8NGA1, Q8NGC7, Q8NGC8, Q8NGC9, Q8NGE0, Q8NGG4, Q8NGI8, Q8NGQ6, Q8NGS4, Q8NGY6, Q8NGY9, Q8NGZ0, Q8NGZ9, Q8NH16, Q8NH74, Q8NHA4, Q8NHB7, Q8NHC8, Q8VEX5, Q8VFR8, Q8VFV4, Q8VFX2, Q8VGI4
Diamond homologs: A3KFT3, A4D2G3, A6NH00, A6NL26, A6NM03, O43869, O76000, O76001, O76002, O95006, O95221, O95371, O95918, P0C7N1, P0C7T2, P23274, P23275, P34984, P59922, Q13606, Q13607, Q5TZ20, Q60880, Q60890, Q6IEZ7, Q6IF00, Q8N127, Q8N349, Q8N628, Q8NG75, Q8NG76, Q8NG77, Q8NG80, Q8NG81, Q8NG83, Q8NG84, Q8NG85, Q8NG97, Q8NGC0, Q8NGE5
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
209 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 198 |
| Likely benign | 7 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
326 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 1:248099353:A:AG | acceptor_gain | 0.9900 |
| 1:248099356:A:AG | acceptor_gain | 0.9900 |
| 1:248099357:G:GA | acceptor_gain | 0.9900 |
| 1:248099354:ACAGT:A | acceptor_loss | 0.9800 |
| 1:248099355:CA:C | acceptor_loss | 0.9800 |
| 1:248099356:A:C | acceptor_loss | 0.9800 |
| 1:248099357:GT:G | acceptor_gain | 0.9700 |
| 1:248099357:GTTAC:G | acceptor_gain | 0.9700 |
| 1:248099354:A:G | acceptor_gain | 0.9600 |
| 1:248099357:GTT:G | acceptor_gain | 0.9600 |
| 1:248099357:GTTA:G | acceptor_gain | 0.9600 |
| 1:248099343:T:G | acceptor_gain | 0.9500 |
| 1:248095195:AAT:A | acceptor_gain | 0.9200 |
| 1:248099482:T:TA | acceptor_gain | 0.9200 |
| 1:248099342:A:AG | acceptor_gain | 0.9000 |
| 1:248098782:G:GT | donor_gain | 0.8900 |
| 1:248099488:C:A | acceptor_gain | 0.8900 |
| 1:248098649:A:AG | acceptor_gain | 0.8800 |
| 1:248098650:G:GG | acceptor_gain | 0.8800 |
| 1:248099355:C:G | acceptor_gain | 0.8600 |
| 1:248099473:T:G | acceptor_gain | 0.8600 |
| 1:248099492:G:A | acceptor_gain | 0.8300 |
| 1:248095195:A:AG | acceptor_gain | 0.8200 |
| 1:248099352:CAACA:C | acceptor_gain | 0.8000 |
| 1:248099562:AGC:A | acceptor_gain | 0.7900 |
| 1:248099353:AACAG:A | acceptor_gain | 0.7800 |
| 1:248099354:ACAG:A | acceptor_gain | 0.7700 |
| 1:248099355:CAG:C | acceptor_gain | 0.7500 |
| 1:248095197:T:TA | acceptor_gain | 0.7300 |
| 1:248099483:G:A | acceptor_gain | 0.7200 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000070318 (1:248066040 G>A), RS1000074814 (1:247937284 G>A,C,T), RS1000076295 (1:247956822 T>A), RS1000084688 (1:247949745 G>A), RS1000114889 (1:248032603 A>G), RS1000117117 (1:248032932 G>T), RS1000128152 (1:248096322 G>A,T), RS1000143677 (1:248018814 C>T), RS1000143768 (1:247989317 T>C), RS1000147238 (1:248016575 G>A,T), RS1000192011 (1:247976585 A>T), RS1000208081 (1:248060682 A>G), RS1000260703 (1:248089570 G>A), RS1000264473 (1:248054437 C>G), RS1000273037 (1:248031580 T>C)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
12 total (human), top 12 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Vehicle Emissions | affects methylation, increases abundance, increases methylation | 2 |
| bisphenol F | decreases methylation, affects cotreatment | 1 |
| bisphenol A | affects methylation, affects cotreatment | 1 |
| 2-palmitoylglycerol | increases expression | 1 |
| bisphenol S | decreases methylation | 1 |
| Fulvestrant | decreases methylation, affects cotreatment, affects methylation | 1 |
| Air Pollutants | affects methylation, increases abundance | 1 |
| Benzo(a)pyrene | affects methylation, decreases methylation | 1 |
| Nitrogen Dioxide | affects methylation, increases abundance | 1 |
| Valproic Acid | decreases methylation | 1 |
| Aflatoxin B1 | decreases methylation | 1 |
| Asbestos, Crocidolite | affects expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.